Human ABCA3, a product of a responsible gene for abca3 for fatal surfactant deficiency in newborns, exhibits unique ATP hydrolysis activity and generates intracellular multilamellar vesicles

This publication has 29 references indexed in Scilit:

• ABCA3Gene Mutations in Newborns with Fatal Surfactant Deficiency
  New England Journal of Medicine, 2004
• Human ABCA7 Supports Apolipoprotein-mediated Release of Cellular Cholesterol and Phospholipid to Generate High Density Lipoprotein
  Journal of Biological Chemistry, 2004
• Functional Interaction between the Two Halves of the Photoreceptor-specific ATP Binding Cassette Protein ABCR (ABCA4)
  Published by Elsevier ,2003
• A Region within a Lumenal Loop of Saccharomyces cerevisiae Ycf1p Directs Proteolytic Processing and Substrate Specificity
  Eukaryotic Cell, 2003
• Effects of Mutations of ABCA1 in the First Extracellular Domain on Subcellular Trafficking and ATP Binding/Hydrolysis
  Journal of Biological Chemistry, 2003
• Requirement of the N-Terminal Extension for Vacuolar Trafficking and Transport Activity of Yeast Ycf1p, an ATP-binding Cassette Transporter
  Molecular Biology of the Cell, 2002
• Introduction: lysosome-related organelles
  Seminars in Cell & Developmental Biology, 2002
• Human ABCA1 Contains a Large Amino-Terminal Extracellular Domain Homologous to an Epitope of Sjögren's Syndrome
  Biochemical and Biophysical Research Communications, 2001
• Primary structure of a novel ABC transporter with a chromosomal localization on the band encoding the multidrug resistance‐associated protein
  FEBS Letters, 1996
• Alteration of the Myometrial Plasma Membrane Cholesterol Content with .beta.-Cyclodextrin Modulates the Binding Affinity of the Oxytocin Receptor
  Biochemistry, 1995